Canonical Allele Identifier: PA2825267048
Gene: DNM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 7286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005362.1:p.Ser615Trp
CA254140
NM_001005362.3:c.1844C>G